AHI1 (NM_001134832) Human 3' UTR Clone

Specifications

Product Data
Product Name	AHI1 (NM_001134832) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AHI-1; dJ71N10.1; JBTS3; ORF1
ACCN	NM_001134832
Insert Size	227 bp
Sequence Data	Insert Sequence (showhide) >SC202460 3’UTR clone of NM_001134832 The sequence shown below is from the reference sequence of NM_001134832. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACATGTATATTATGGTGGAAAAAGCACTAGACTCAGGGTCAGCCAGCCAGAAGAACTGAGCCGACCTGG GATCCCACCACTTCCTAACTGTTTTGTTAGGTAGTTCACTTTCTCTCTTCGGATAAATGTCTCCACATT TCCTACTTCATAGAATTGTCAGAATCAACACAATACATTTAATACTTTGAAACTCATAAAATATTGGGA GAATAAACAGTATGAGGTTA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_001134832.2
Synonyms	AHI-1; dJ71N10.1; JBTS3; ORF1
Summary	This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]
Locus ID	54806
MW	8.8

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